{{Rsnum
|rsid=121918603
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=RYR2
|position=237639068
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RYR2
}}{{omim
|id=180902
|rsnum=121918603
|variant=0007
}}{{ClinVar
|rsid=121918603
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=237639068
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000a05000002110100
|GENEINFO=RYR2:6262
|GENE_NAME=RYR2
|GENE_ID=6262
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.237639068C>T
|CLNSRC=ClinVar; GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_001035.2:c.6982C>T; NBK1289; 180902.0007
|CLNSIG=5
|CLNCUI=C1631597
|CLNDBN=Catecholaminergic polymorphic ventricular tachycardia
|Disease=Catecholaminergic polymorphic ventricular tachycardia
|CLNACC=RCV000013826.22
|Tags=PM;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1289:C1631597:604772:ORPHA3286:419671004
}}